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Compound Detail

CHEMBL3335522

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CC(C)(C)[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)c1ccc(/C=C2\SC(=O)N(C3CCCC3)C2=O)cc1)C(N)=O

Basic Information

ChEMBL ID CHEMBL3335522
Phase Preclinical
Structure Type MOL
InChI Key QHZOMZDAMAEAJS-DJVUMTHLSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

713.9
MW (Da)
1.66
ALogP
9
HBA
8
HBD
255.7
PSA (Ų)
0.05
QED
2
Ro5 Violations
17
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C34H51N9O6S
MW 713.91
Aromatic Rings 1
Heavy Atoms 50
NP-Likeness -0.21

Activity Summary

IC50 1 meas. best 4.53

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Genome polyprotein
CHEMBL3308998
IC50 4.53 4.53 29800.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Genome polyprotein IC50 = 29800.0 nM 4.53 Inhibition of Dengue virus serotype 2 NS2B-NS3 protease by homogeneous fluorimet... 25221663

Literature References

PubMed DOI Target Context # Activities
25221663 10.1021/ml500245v Genome polyprotein 3
25221663 10.1021/ml500245v Prothrombin 1

Data from ChEMBL 36 via Core Engine